DBA9
MCID: DMN022
MIFTS: 28

Diamond-Blackfan Anemia 9 (DBA9)

Categories: Blood diseases, Bone diseases, Fetal diseases, Genetic diseases, Immune diseases, Metabolic diseases, Rare diseases

Aliases & Classifications for Diamond-Blackfan Anemia 9

MalaCards integrated aliases for Diamond-Blackfan Anemia 9:

Name: Diamond-Blackfan Anemia 9 57 12 73 29 13 6 44 15 71
Dba9 57 12 73
Rps10-Related Diamond-Blackfan Anemia 12
Anemia, Diamond-Blackfan, Type 9 39

Characteristics:

OMIM®:

57 (Updated 05-Mar-2021)
Inheritance:
autosomal dominant

Miscellaneous:
limited clinical information provided
some patients are steroid responsive
age at diagnosis ranged from birth to 12 years


HPO:

31
diamond-blackfan anemia 9:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

Disease Ontology 12 DOID:0111884
OMIM® 57 613308
OMIM Phenotypic Series 57 PS105650
MedGen 41 C2750081
UMLS 71 C2750081

Summaries for Diamond-Blackfan Anemia 9

OMIM® : 57 Diamond-Blackfan anemia (DBA) is an inherited red blood cell aplasia that usually presents in the first year of life. The main features are normochromic macrocytic anemia, reticulocytopenia, and nearly absent erythroid progenitors in the bone marrow. Patients show growth retardation, and approximately 30 to 50% have craniofacial, upper limb, heart, and urinary system congenital malformations. The majority of patients have increased mean corpuscular volume, elevated erythrocyte adenosine deaminase activity, and persistence of hemoglobin F. However, some DBA patients do not exhibit these findings, and even in the same family, symptoms can vary between affected family members (summary by Landowski et al., 2013). For a discussion of genetic heterogeneity of Diamond-Blackfan anemia, see DBA1 (105650). (613308) (Updated 05-Mar-2021)

MalaCards based summary : Diamond-Blackfan Anemia 9, also known as dba9, is related to diamond-blackfan anemia and diamond-blackfan anemia 1. An important gene associated with Diamond-Blackfan Anemia 9 is RPS10 (Ribosomal Protein S10). Affiliated tissues include bone marrow, and related phenotypes are webbed neck and anemia

Disease Ontology : 12 A Diamond-Blackfan anemia that has material basis in heterozygous mutation in RPS10 on chromosome 6p21.31.

UniProtKB/Swiss-Prot : 73 Diamond-Blackfan anemia 9: A form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond- Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre- Robin syndrome and cleft palate), thumb and urogenital anomalies.

Related Diseases for Diamond-Blackfan Anemia 9

Symptoms & Phenotypes for Diamond-Blackfan Anemia 9

Human phenotypes related to Diamond-Blackfan Anemia 9:

31
# Description HPO Frequency HPO Source Accession
1 webbed neck 31 occasional (7.5%) HP:0000465
2 anemia 31 HP:0001903
3 growth delay 31 HP:0001510
4 low levels of vitamin d 31 HP:0100512

Symptoms via clinical synopsis from OMIM®:

57 (Updated 05-Mar-2021)
Hematology:
anemia

Laboratory Abnormalities:
vitamin d deficiency

Head And Neck Neck:
webbed neck (rare)

Growth Other:
growth retardation

Head And Neck Face:
cathie facies

Clinical features from OMIM®:

613308 (Updated 05-Mar-2021)

GenomeRNAi Phenotypes related to Diamond-Blackfan Anemia 9 according to GeneCards Suite gene sharing:

26
# Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 Increased shRNA abundance (Z-score > 2) GR00366-A-213 9.8 RPS10 RPS10-NUDT3
2 Increased shRNA abundance (Z-score > 2) GR00366-A-81 9.8 RPS10 RPS10-NUDT3
3 Increased shRNA abundance (Z-score > 2) GR00366-A-87 9.8 RPS10 RPS10-NUDT3
4 Decreased shRNA abundance (Z-score < -2) GR00366-A-11 9.65 RPS10 RPS10-NUDT3
5 Decreased shRNA abundance (Z-score < -2) GR00366-A-177 9.65 RPS10 RPS10-NUDT3
6 Decreased shRNA abundance (Z-score < -2) GR00366-A-29 9.65 RPS10 RPS10-NUDT3
7 Decreased shRNA abundance (Z-score < -2) GR00366-A-72 9.65 RPS10 RPS10-NUDT3
8 Decreased shRNA abundance (Z-score < -2) GR00366-A-73 9.65 RPS10 RPS10-NUDT3

Drugs & Therapeutics for Diamond-Blackfan Anemia 9

Search Clinical Trials , NIH Clinical Center for Diamond-Blackfan Anemia 9

Cochrane evidence based reviews: diamond-blackfan anemia 9

Genetic Tests for Diamond-Blackfan Anemia 9

Genetic tests related to Diamond-Blackfan Anemia 9:

# Genetic test Affiliating Genes
1 Diamond-Blackfan Anemia 9 29 RPS10

Anatomical Context for Diamond-Blackfan Anemia 9

MalaCards organs/tissues related to Diamond-Blackfan Anemia 9:

40
Bone Marrow

Publications for Diamond-Blackfan Anemia 9

Articles related to Diamond-Blackfan Anemia 9:

# Title Authors PMID Year
1
Target enrichment and high-throughput sequencing of 80 ribosomal protein genes to identify mutations associated with Diamond-Blackfan anaemia. 57 6
23718193 2013
2
Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia. 57 6
20116044 2010
3
Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia. 57
23812780 2013

Variations for Diamond-Blackfan Anemia 9

ClinVar genetic disease variations for Diamond-Blackfan Anemia 9:

6 (show all 22)
# Gene Name Type Significance ClinVarId dbSNP ID GRCh37 Pos GRCh38 Pos
1 RPS10-NUDT3 NM_001014.5(RPS10):c.3G>A (p.Met1Ile) SNV Pathogenic 6185 rs267607021 6:34392996-34392996 6:34425219-34425219
2 RPS10-NUDT3 NM_001014.5(RPS10):c.260dup (p.Glu88fs) Duplication Pathogenic 6186 rs1581931541 6:34392507-34392508 6:34424730-34424731
3 RPS10-NUDT3 NM_001014.5(RPS10):c.337C>T (p.Arg113Ter) SNV Pathogenic 6187 rs267607022 6:34389570-34389570 6:34421793-34421793
4 RPS10-NUDT3 NM_001014.5(RPS10):c.364G>A (p.Ala122Thr) SNV Uncertain significance 356420 rs886061322 6:34389543-34389543 6:34421766-34421766
5 RPS10-NUDT3 NM_001014.5(RPS10):c.*25G>T SNV Uncertain significance 356418 rs886061321 6:34385258-34385258 6:34417481-34417481
6 RPS10-NUDT3 NM_001014.5(RPS10):c.322+2_322+4dup Duplication Uncertain significance 225461 rs1554164160 6:34392441-34392442 6:34424664-34424665
7 RPS10-NUDT3 NM_001014.5(RPS10):c.168C>T (p.Gly56=) SNV Uncertain significance 906571 6:34392600-34392600 6:34424823-34424823
8 RPS10-NUDT3 NM_001014.5(RPS10):c.-9G>C SNV Uncertain significance 907588 6:34393817-34393817 6:34426040-34426040
9 RPS10-NUDT3 NM_001014.5(RPS10):c.-27C>A SNV Uncertain significance 907589 6:34393835-34393835 6:34426058-34426058
10 RPS10-NUDT3 NM_001014.5(RPS10):c.6G>A (p.Leu2=) SNV Likely benign 356423 rs146246722 6:34392993-34392993 6:34425216-34425216
11 RPS10-NUDT3 NM_001014.5(RPS10):c.111C>G (p.Asp37Glu) SNV Likely benign 356421 rs374314919 6:34392888-34392888 6:34425111-34425111
12 RPS10-NUDT3 NM_001014.5(RPS10):c.71A>G (p.Lys24Arg) SNV Likely benign 356422 rs201147592 6:34392928-34392928 6:34425151-34425151
13 RPS10-NUDT3 NM_001014.5(RPS10):c.-37C>T SNV Benign 356431 rs9469779 6:34393845-34393845 6:34426068-34426068
14 RPS10-NUDT3 NM_001014.5(RPS10):c.-29C>T SNV Benign 356428 rs140822093 6:34393837-34393837 6:34426060-34426060
15 RPS10-NUDT3 NM_001014.5(RPS10):c.-21C>G SNV Benign 356427 rs181470609 6:34393829-34393829 6:34426052-34426052
16 RPS10-NUDT3 NM_001014.5(RPS10):c.*43A>G SNV Benign 356417 rs200231286 6:34385240-34385240 6:34417463-34417463
17 RPS10-NUDT3 NM_001014.5(RPS10):c.1-3C>G SNV Benign 356424 rs375500787 6:34393001-34393001 6:34425224-34425224
18 RPS10-NUDT3 NM_001014.5(RPS10):c.-14C>T SNV Benign 356426 rs576997899 6:34393822-34393822 6:34426045-34426045
19 RPS10-NUDT3 NM_001014.5(RPS10):c.437C>T (p.Ser146Leu) SNV Benign 904984 6:34386165-34386165 6:34418388-34418388
20 RPS10-NUDT3 NM_001014.5(RPS10):c.432T>G (p.Ala144=) SNV Benign 906570 6:34386170-34386170 6:34418393-34418393
21 RPS10-NUDT3 NM_001014.5(RPS10):c.408C>T (p.Ala136=) SNV Benign 356419 rs147566753 6:34386194-34386194 6:34418417-34418417
22 RPS10-NUDT3 NM_001014.5(RPS10):c.231G>A (p.Gln77=) SNV Benign 238211 rs147863199 6:34392537-34392537 6:34424760-34424760

Expression for Diamond-Blackfan Anemia 9

Search GEO for disease gene expression data for Diamond-Blackfan Anemia 9.

Pathways for Diamond-Blackfan Anemia 9

GO Terms for Diamond-Blackfan Anemia 9

Cellular components related to Diamond-Blackfan Anemia 9 according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 ribosome GO:0005840 8.62 RPS10-NUDT3 RPS10

Sources for Diamond-Blackfan Anemia 9

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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